10PC - UP - 380-54620 - Locamotive

Primary DI: 00766588110127
Brand: 10PC - UP - 380-54620 - Locamotive
Company: Certified Safety Manufacturing, Inc.
Model: K611-012
Catalog number: K611-012
Device description: 10PC - UP - 380-54620 - Locamotive
Published: 2022-07-15
Public version status: New
Distribution status: In Commercial Distribution
MRI safety: Labeling does not contain MRI Safety Information
Rx: false
OTC: false
Sterile: false
Single use: true

Related Records

Contact Domains

certifiedsafety.com

Product Codes

Code	Name
EFQ	GAUZE/SPONGE, INTERNAL

Product Code Classifications

Code	Device	Specialty	Class
EFQ	Gauze/Sponge, Internal	Unknown	U

Identifiers And Packaging

Identifier	Type	Agency	Package quantity	Status
00766588110127	Primary	GS1	0

Alternate GTIN / UPC / EAN Codes

Source identifier	GTIN-14 normalized	UPC-A	EAN-13
00766588110127	00766588110127	766588110127	0766588110127

GMDN Terms

Term	Definition
Wound-nonadherent dressing, absorbent, non-antimicrobial	A wound covering typically in the form of a multi-layered pad having a material or substance on its skin-contact surface (e.g., silicone gel), or designed to be soaked in saline prior to application, to prevent adherence to the wound bed thereby decreasing wound trauma potential; it does not contain an antimicrobial agent. It is typically used to absorb wound blood/exudates while protecting the wound from external contamination and maintaining a moist internal environment. It may be used as a primary or secondary dressing to treat chronic and postoperative wounds, burns, ulcers, abrasions, cuts, or puncture sites; it is not a dedicated burn dressing. This is a single-use device.

Term

Definition

Wound-nonadherent dressing, absorbent, non-antimicrobial

A wound covering typically in the form of a multi-layered pad having a material or substance on its skin-contact surface (e.g., silicone gel), or designed to be soaked in saline prior to application, to prevent adherence to the wound bed thereby decreasing wound trauma potential; it does not contain an antimicrobial agent. It is typically used to absorb wound blood/exudates while protecting the wound from external contamination and maintaining a moist internal environment. It may be used as a primary or secondary dressing to treat chronic and postoperative wounds, burns, ulcers, abrasions, cuts, or puncture sites; it is not a dedicated burn dressing. This is a single-use device.

Sterilization Methods

Method

Contacts

Phone	Email
+1(816)483-9090	Info@certifiedsafety.com

Regulatory Flags

DUNS number: 788460483
Device count: 1
DM exempt: false
Premarket exempt: false
HCT/P: false
Kit: false
Combination product: false
Lot or batch: true
Serial number: false
Manufacturing date on label: false
Expiration date on label: false
Donation ID number: false
Contains natural rubber latex: false
No natural rubber latex: false
Sterilization required before use: false

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